Recalls affecting North Dakota
Notices that name North Dakota in their distribution area, plus every nationwide recall — nationwide recalls reach North Dakota too.
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Class II · 1+ years ago
Cardinal Health 200, LLC Salem Sump PVC Tubes: Product Code/Product Name: 264929 recall: Firm has received complaints regarding Anti-Reflux Valve (ARV) breakage
Firm has received complaints regarding Anti-Reflux Valve (ARV) breakage due to excessive force during use. Firm is providing additional guidance for…
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Class II · 1+ years ago
Cardinal Health 200, LLC Salem Sump PVC Tubes: Product Code/Product Name: 8888265108 recall: Firm has received complaints regarding Anti-Reflux Valve (ARV) breakage
Firm has received complaints regarding Anti-Reflux Valve (ARV) breakage due to excessive force during use. Firm is providing additional guidance for…
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Class II · 1+ years ago
Baxter Healthcare Corporation Oral Probe , accessory used with Welch Allyn SureTemp recall: Affected oral/axillary probes were inadvertently programmed with the rectal
Affected oral/axillary probes were inadvertently programmed with the rectal probe configuration. Affected probes will potentially display a lower…
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Class II · 1+ years ago
Medline Industries, LP Excelsior Medical, 0.9% Sodium Chloride Injection recall: Medline has identified a limited quantity of saline IV flush syringes
Medline has identified a limited quantity of saline IV flush syringes that may not meet the required concentration of sodium chloride.
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Class II · 1+ years ago
Bristol-Myers Squibb Company Opdualag injection, 240 mg and 80 mg/20 mL recall: Lack of Assurance of Sterility
Lack of Assurance of Sterility.
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Class II · 1+ years ago
Aspiro Pharma Limited Ketorolac Tromethamine Injection, USP, 60 mg/2 mL recall: Presence of Particulate Matter: Particulate matter identified as glass
Presence of Particulate Matter: Particulate matter identified as glass
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Class II · 1+ years ago
Church & Dwight Co., Inc. Zicam" Medicated Fruit Drops Elderberry Flavor recall: Labeling: Label Mix-up: The product in the bottle contains elderberry
Labeling: Label Mix-up: The product in the bottle contains elderberry and the label failed to indicate the inclusion of elderberry as an ingredient.
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Class III · 1+ years ago
JB Chemicals and Pharmaceuticals Ltd Cetirizine Hydrochloride Tablets USP 10 mg recall: Tablet/Capsules Imprinted with Wrong ID
Tablet/Capsules Imprinted with Wrong ID
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Class II · 1+ years ago
The Harvard Drug Group LLC Gabapentin Capsules, USP, 100 mg, 100 Capsules recall: Failed Impurities/Degradation Specifications: an out of specification result
Failed Impurities/Degradation Specifications: an out of specification result obtained during routine stability testing for Highest Unknown Impurity .
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Class II · 1+ years ago
Medline, Alcohol Prep Pads , 100 eaches per box recall: Subpotent Drug
Subpotent Drug
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Class II · 1+ years ago
USV Private Limited Olopatadine Hydrochloride Ophthalmic Solution USP 0.1 % recall: Failed Impurities/Degradation Specifications: The result for 'Any individual
Failed Impurities/Degradation Specifications: The result for 'Any individual unspecified impurity' exceeds the specification limit.
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Class III · 1+ years ago
JB Chemicals and Pharmaceuticals Ltd Cetirizine Hydrochloride Tablets USP 10 mg recall: Tablet/Capsules Imprinted with Wrong ID
Tablet/Capsules Imprinted with Wrong ID
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Class II · 1+ years ago
The Harvard Drug Group LLC Gabapentin Capsules, USP, 100 mg, 10 Capsules recall: Failed Impurities/Degradation Specifications: an out of specification result
Failed Impurities/Degradation Specifications: an out of specification result obtained during routine stability testing for Highest Unknown Impurity .
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Class II · 1+ years ago
Lannett Company Inc. Niacin Extended-release Tablets, USP, 1,000 mg recall: Failed Dissolution Specifications
Failed Dissolution Specifications
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Class II · 1+ years ago
Graviti Pharmaceuticals Private Limited Bupropion Hydrochloride Extended-Release recall: Failed Tablet/Capsule Specifications
Failed Tablet/Capsule Specifications
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Class I · 1+ years ago
M.C.I. Foods, Inc. Cheese and Egg with Green Salsa Breakfast Burrito recall: Cooked egg ingredient for Ready-to-Eat products tested positive for Listeria
Cooked egg ingredient for Ready-to-Eat products tested positive for Listeria Monocytogenes
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Class I · 1+ years ago
M.C.I. Foods, Inc. Egg and Cheese Breakfast Burrito recall: Cooked egg ingredient for Ready-to-Eat products tested positive for Listeria
Cooked egg ingredient for Ready-to-Eat products tested positive for Listeria Monocytogenes
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High - Class I · 1+ years ago
E.A. Sween Company Pulled Pork Sandwich products recall: Product Contamination
Product Contamination
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High - Class I · 1+ years ago
Hormel Foods Corporation Ready-To-Eat Frozen Chicken products recall: Product Contamination
Product Contamination
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NHTSA safety recall · 1+ years ago
Ford recall: The windshield glass may have visible air bubbles
The windshield glass may have visible air bubbles, which can obscure the driver's visibility. As such, these vehicles fail to comply with the…
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High - Class I · 1+ years ago
LSI, Inc. BBQ Pork Jerky products recall: Product Contamination
Product Contamination
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NHTSA safety recall · 1+ years ago
Chrysler Ram ProMaster recall: The electrical circuit for the radiator fan may overheat
The electrical circuit for the radiator fan may overheat.
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NHTSA safety recall · 1+ years ago
Honda CB1000SP Hornet SP recall: The pivot bolt on the gearshift pedal may loosen and detach
The pivot bolt on the gearshift pedal may loosen and detach, resulting in the inability to shift gears. As such, these motorcycles fail to comply…
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Elevated risk · 1+ years ago
Sauna360 Tylö Halmstad and Kiruna Hybrid Saunas recall: Fall Hazard
Fall Hazard